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   <subfield code="a">Prevalence of blaZ gene types and the cefazolin inoculum effect among methicillin-susceptible Staphylococcus aureus blood isolates and their association with multilocus sequence types and clinical outcome</subfield>
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   <subfield code="c">[Y. Chong, S.‐J. Park, E. Kim, K.-M. Bang, M.-N. Kim, S.-H. Kim, S.-O. Lee, S.-H. Choi, J.-Y. Jeong, J. Woo, Y. Kim]</subfield>
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   <subfield code="a">Cefazolin treatment failures have been described for bacteraemia caused by methicillin-susceptible Staphylococcus aureus (MSSA) with type A β-lactamase and inoculum effect (InE). We investigated the prevalence of blaZ (β-lactamase) gene types and a cefazolin InE among MSSA blood isolates in South Korea and evaluated their association with specific genotypes. The clinical impact of the cefazolin InE was also evaluated. A total of 220 MSSA isolates were collected from a prospective cohort study of S. aureus bacteraemia. A pronounced InE with cefazolin was defined as a ≥4-fold increase in the minimum inhibitory concentration (MIC) between a standard and high inoculum, resulting in a non-susceptible MIC. Sequencing of blaZ and multilocus sequence typing (MLST) were performed. Clinical outcomes were assessed in 77 patients treated with cefazolin. The blaZ gene was detected in 92% of the 220 MSSA isolates. Type C β-lactamase was the most common (53%), followed by type B (20%) and type A (17%). Certain genotypes were significantly associated with specific β-lactamase types (notably, ST30 and type A β-lactamase). A pronounced cefazolin InE was observed in 13% of isolates. Most of these (79%) expressed type A β-lactamase and ST30 was the predominant (55%) clone amongst them. Cefazolin treatment failure was not observed in patients infected with strains exhibiting a pronounced InE. These strains had no impact on other clinical outcomes. In conclusion, the prevalence of a pronounced InE with cefazolin could be dependent upon distributions of MSSA genotypes. Cefazolin can likely be used for the treatment of MSSA bacteraemia (except endocarditis), without consideration of an InE.</subfield>
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   <subfield code="D">Y.</subfield>
   <subfield code="u">Department of Infectious Diseases, Asan Medical Center, University of Ulsan College of Medicine, 88, Olympic-ro 43-gil, 138-736, Songpa-gu, Seoul, Republic of Korea</subfield>
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   <subfield code="u">Department of Infectious Diseases, Asan Medical Center, University of Ulsan College of Medicine, 88, Olympic-ro 43-gil, 138-736, Songpa-gu, Seoul, Republic of Korea</subfield>
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